Variant report

Variant	rs34931002
Chromosome Location	chr19:18811048-18811049
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:18793196..18796069-chr19:18810144..18811695,2	K562	blood:
2	chr19:18810589..18812335-chr19:18824171..18827003,2	MCF-7	breast:
3	chr19:18777019..18779428-chr19:18809740..18812402,2	K562	blood:
4	chr19:18810890..18813557-chr19:18875190..18876829,2	K562	blood:
5	chr19:18789026..18790711-chr19:18810926..18813520,2	K562	blood:
6	chr19:18653429..18654988-chr19:18810315..18813230,2	K562	blood:
7	chr19:18809327..18811934-chr19:18826162..18828018,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000105701	Chromatin interaction
ENSG00000105662	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11670024	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11672177	0.82[AMR][1000 genomes]
rs12973480	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12980791	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13344506	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17683623	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35212572	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7253058	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv911286	chr19:18652844-18811112	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv911289	chr19:18700047-18811112	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	esv3393439	chr19:18807352-18811750	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv960927	chr19:18808010-18837082	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18795400-18811400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr19:18795400-18811400	Weak transcription	NH-A	brain
3	chr19:18795800-18811400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:18795800-18811400	Weak transcription	Fetal Lung	lung
5	chr19:18795800-18811400	Weak transcription	Right Atrium	heart
6	chr19:18796200-18811200	Weak transcription	Fetal Brain Female	brain
7	chr19:18797200-18811200	Weak transcription	NHLF	lung
8	chr19:18797200-18822400	Weak transcription	HepG2	liver
9	chr19:18808000-18811600	Weak transcription	Fetal Kidney	kidney
10	chr19:18808000-18811600	Enhancers	Stomach Mucosa	stomach
11	chr19:18808400-18811400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr19:18808400-18811400	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr19:18808600-18811600	Weak transcription	Psoas Muscle	Psoas
14	chr19:18809000-18811400	Enhancers	Fetal Muscle Leg	muscle
15	chr19:18809200-18811400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr19:18809200-18811400	Enhancers	Esophagus	oesophagus
17	chr19:18809200-18811400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr19:18809400-18811400	Enhancers	Pancreas	Pancrea
19	chr19:18809400-18811600	Enhancers	Spleen	Spleen
20	chr19:18809600-18811400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr19:18809600-18811400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr19:18809600-18811400	Enhancers	Fetal Thymus	thymus
23	chr19:18809600-18811400	Enhancers	Dnd41	blood
24	chr19:18809600-18811600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:18809600-18811600	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr19:18809800-18811200	Flanking Active TSS	Primary T cells from cord blood	blood
27	chr19:18809800-18811600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr19:18810000-18811400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr19:18810000-18811400	Enhancers	HMEC	breast
30	chr19:18810000-18811600	Weak transcription	Gastric	stomach
31	chr19:18810200-18811200	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr19:18810200-18811400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr19:18810200-18811400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr19:18810200-18811400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr19:18810200-18811400	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr19:18810200-18811400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr19:18810200-18811400	Enhancers	K562	blood
38	chr19:18810200-18811600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr19:18810200-18812400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr19:18810200-18812400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr19:18810400-18811200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr19:18810400-18811200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr19:18810400-18811200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr19:18810400-18811200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
45	chr19:18810400-18811200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
46	chr19:18810400-18811400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr19:18810400-18811400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr19:18810400-18811600	Enhancers	Placenta	Placenta
49	chr19:18810400-18812400	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr19:18810400-18812400	Flanking Active TSS	GM12878-XiMat	blood

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